Metallothionein: An intracellular protein to protect against cadmium toxicity

被引:919
作者
Klaassen, CD [1 ]
Liu, J [1 ]
Choudhuri, S [1 ]
机构
[1] Univ Kansas, Med Ctr, Dept Pharmacol, Ctr Environm Hlth & Occupat Med, Kansas City, KS 66160 USA
关键词
MT-transgenic and knockout animals; cadmium; zinc; free radical scavenge;
D O I
10.1146/annurev.pharmtox.39.1.267
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Metallothioneins (MT) are low-molecular-weight, cysteine-rich, metal-binding proteins. MT genes are readily induced by various physiologic and toxicologic stimuli. Because the cysteines in MT are absolutely conserved across species, it was suspected that the cysteines are necessary for function and MT is essential for Life. In attempts to determine the function(s) of MT, studies have been performed using four different experimental paradigms: (a) animals injected with chemicals known to induce MT; (b) cells adapted to survive and grow in high concentrations of MT-inducing toxicants; (c) cells transfected with the MT gene; and (d) MT-transgenic and MT-null mice. Most often, results from studies using the first three approaches have indicated multiple functions of MT in cell biology: MT (a) is a "storehouse" for zinc, (b) is a free-radical scavenger, and (c) protects against cadmium (Cd) toxicity. However, studies using MT-transgenic and null mice have not strongly supported the first two proposed functions but strongly support its function in protecting against Cd toxicity. Repeated administration of Cd to MT-null mice results in nephrotoxicity at one tenth the dose that produces nephrotoxicity in control mice. Human studies indicate that 7% of the general population have renal dysfunction from Cd exposure. Therefore, if humans did not have MT, "normal" Cd exposure would be nephrotoxic to humans. Thus, it appears that during evolution, the ability of MT to protect against Cd toxicity might have taken a more pivotal role in the maintenance of life processes, as compared with its other proposed functions (i.e. storehouse for zinc and free radical scavenger).
引用
收藏
页码:267 / 294
页数:28
相关论文
共 205 条
[1]   INHIBITION OF HYDROXYL-RADICAL-GENERATED DNA-DEGRADATION BY METALLOTHIONEIN [J].
ABEL, J ;
DERUITER, N .
TOXICOLOGY LETTERS, 1989, 47 (02) :191-196
[2]   Regulation of metallothionein-III (GIF) mRNA in the brain of patients with Alzheimer disease is not impaired [J].
Amoureux, MC ;
Van Gool, D ;
Herrero, MT ;
Dom, R ;
Colpaert, FC ;
Pauwels, PJ .
MOLECULAR AND CHEMICAL NEUROPATHOLOGY, 1997, 32 (1-3) :101-121
[3]  
ANDREWS GK, 1990, PROG FOOD NUTR SCI, V14, P193
[4]  
Apostolova MD, 1997, J TRACE ELEM MED BIO, V11, P1
[5]   Metallothioneins in brain - The role in physiology and pathology [J].
Aschner, M ;
Cherian, MG ;
Klaassen, CD ;
Palmiter, RD ;
Erickson, JC ;
Bush, AI .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1997, 142 (02) :229-242
[6]   INDUCTION OF HEPATIC METALLOTHIONEIN BY PARAQUAT [J].
BAUMAN, JW ;
MADHU, C ;
MCKIM, JM ;
LIU, YP ;
KLAASSEN, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 117 (02) :233-241
[7]   INCREASE IN METALLOTHIONEIN PRODUCED BY CHEMICALS THAT INDUCE OXIDATIVE STRESS [J].
BAUMAN, JW ;
LIU, J ;
LIU, YP ;
KLAASSEN, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1991, 110 (02) :347-354
[8]   INDUCTION OF METALLOTHIONEIN BY DIETHYL MALEATE [J].
BAUMAN, JW ;
MCKIM, JM ;
LIU, J ;
KLAASSEN, CD .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 114 (02) :188-196
[9]  
BHATTACHARYYA MH, 1998, METALLOTHIONEIN, V4, P473
[10]   Physiologic function of the Wilson disease gene product, ATP7B [J].
Bingham, MJ ;
Ong, TJ ;
Summer, KH ;
Middleton, RB ;
McArdle, HJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1998, 67 (05) :982S-987S